0000000001303113

AUTHOR

Marc Sallé

showing 16 related works from this author

Tuning the electronic properties and the planarity degree in the π-extended TTF series: the prominent role of heteroatoms

2018

The main asset of small molecules for application in organic electronics lies in the tunability of their electronic properties owing to the precise control of their molecular design. Semiconducting properties in organic compounds are for instance closely linked to the molecular planarity degree, including when considering various redox states. Among those species, the π-extended TTF (exTTF: 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene) presents fascinating redox and structural properties, which have been extensively studied in various fields of organic electronics. Here we show that S-exTTF, a sulfur enriched π-isoelectronic dithieno analogue of pristine exTTF, synthesized through…

Organic electronicsMaterials scienceHeteroatom02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSmall moleculeRedoxPlanarity testing0104 chemical sciencesCrystallographysymbols.namesakeIntramolecular forceMaterials Chemistrysymbols[CHIM]Chemical SciencesVan der Waals radiusCyclic voltammetry0210 nano-technologyComputingMilieux_MISCELLANEOUS
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π conjugation across the tetrathiafulvalene core: Synthesis of extended tetrathiafulvalene derivatives and theoretical analysis of their unusual elec…

2000

A series of extended tetrathiafulvalene (TTF) derivatives bearing one or two 1,4-dithiafulven-6-yl substitutents has been prepared. The new compounds present remarkable electrochemical singularities compared with other TTF derivatives, which are strongly affected by the nature of the substitution on the lateral heterocycle(s). This unusual electrochemical behaviour follows a square-scheme sequence and is attributed to structural changes upon oxidation of the pi-donating molecules. Digital simulations of the electrochemical data have been used to reach the values of the kinetic and thermodynamic constants involved in the square scheme. Theoretical calculations establish an important contribu…

Pi systemOrganic ChemistryInorganic chemistryNonlinear opticsGeneral ChemistryConjugated systemElectrochemistryCatalysischemistry.chemical_compoundCrystallographychemistryAb initio quantum chemistry methodsMoleculeCyclic voltammetryTetrathiafulvalene
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Controlling the Host-Guest Interaction Mode through a Redox Stimulus

2017

International audience; A proof-of-concept related to the redox-control of the binding/releasing process in a host-guest system is achieved by designing a neutral and robust Pt-based redox-active metallacage involving two extended-tetrathiafulvalene (exTTF) ligands. When neutral, the cage is able to bind a planar polyaromatic guest (coronene). Remarkably, the chemical or electrochemical oxidation of the host-guest complex leads to the reversible expulsion of the guest outside the cavity, which is assigned to a drastic change of the host-guest interaction mode, illustrating the key role of counteranions along the exchange process. The reversible process is supported by various experimental d…

010405 organic chemistryStereochemistrySupramolecular chemistryGeneral MedicineGeneral ChemistryReversible processself-assembly010402 general chemistryElectrochemistry01 natural sciencesRedoxsupramolecular cageCatalysisCoronene0104 chemical scienceschemistry.chemical_compoundchemistryChemical physicsDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySelf-assemblyTetrathiafulvaleneexTTF
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First signals of electrochemically oxidized species of TTF and TMT-TTF : a study by in situ spectroelectrochemical FTIR and DFT calculations

2003

A first study by in situ FTIR spectroelectrochemistry of TTF and TTM-TTF has been undertaken. The oxidation, in this case, is caused only by electrochemistry, which constitutes a clear advantage over chemical oxidation since no side products are present in the solution. In this context, we obtained the signals of neutral, radical cation, and dication species of TTF and TTM-TTF. The experimental conditions were chosen in order to avoid the possible formation of π-dimer species and to obtain a satisfactory signal-to-noise ratio. A weak signal was detected for TTF and a stronger one for TTM-TTF. The changes induced by the oxidation process in the IR spectra of TTF and TTM-TTF have been analyze…

Analytical chemistryGeneral Physics and AstronomyInfrared spectroscopyContext (language use)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesFourier transform spectroscopy0104 chemical sciencesDicationchemistry.chemical_compoundRadical ionchemistryPhysical chemistryDensity functional theoryPhysical and Theoretical Chemistry0210 nano-technologyTetrathiafulvalene
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O-Doped Nanographenes: A Pyrano/Pyrylium Route Towards Semiconducting Cationic Mixed-Valence Complexes

2020

Herein we report an efficient synthesis to prepare O‐doped nanographenes, which derive from the longitudinally and latitudinally p‐extension of pyrene. The derivatives are highly fluorescent and feature low‐oxidation potentials. Exploiting electrooxidation, crystals of cationic mixed valence (MV) complexes were grown in which the organic salts organize into face‐to‐face p‐ p stacks, a favorable solid‐state arrangement for organic electronics. Variable‐temperature EPR measurements and relaxation studies suggest a strong electron delocalization along the longitudinal axis of the columnar p‐stacking architectures. Electric measurements of single crystals of the MV salts exhibited a semiconduct…

Materials sciencemolecular graphenespolycyclic aromatic hydrocarbonsHeteroatom010402 general chemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundCompostos orgànicslaw[CHIM]Chemical ScienceselectrocrystallizationElectron paramagnetic resonanceOrganic electronicsValence (chemistry)[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryDopingCationic polymerizationGeneral MedicineGeneral Chemistryelectrocrystallization; electron paramagnetic resonance; heteroatom doping; molecular graphenes; polycyclic aromatic hydrocarbonsFluorescence0104 chemical sciencesElectroquímicaCrystallographyelectron paramagnetic resonancechemistryPyreneheteroatom doping
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CCDC 1557895: Experimental Crystal Structure Determination

2020

Related Article: Luka Ðorđević, Cataldo Valentini, Nicola Demitri, Cécile Mézière, Magali Allain, Marc Sallé, Andrea Folli, Damien Murphy, Samuel Mañas-Valero, Eugenio Coronado, Davide Bonifazi|2020|Angew.Chem.,Int.Ed.|59|4106|doi:10.1002/anie.201914025

3813-tri-t-butyl[1]benzopyrano[4'3'2':110]phenanthro[345-mnab]xanthene dibromomethane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1920493: Experimental Crystal Structure Determination

2020

Related Article: Luka Ðorđević, Cataldo Valentini, Nicola Demitri, Cécile Mézière, Magali Allain, Marc Sallé, Andrea Folli, Damien Murphy, Samuel Mañas-Valero, Eugenio Coronado, Davide Bonifazi|2020|Angew.Chem.,Int.Ed.|59|4106|doi:10.1002/anie.201914025

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters16-bis(4-t-butyl-2-methoxyphenyl)pyreneExperimental 3D Coordinates
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CCDC 1834564: Experimental Crystal Structure Determination

2018

Related Article: Serhii Krykun, Vincent Croué, Magali Allain, Zoia Voitenko, Juan Aragó, Enrique Ortí, Sébastien Goeb, Marc Sallé|2018|J.Mater.Chem.C|6|13190|doi:10.1039/C8TC04730H

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters48-bis[45-bis(methylsulfanyl)-2H-13-dithiol-2-ylidene]-48-dihydrobenzo[12-b:45-b']bisthiophene dichloromethane solvateExperimental 3D Coordinates
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CCDC 1557896: Experimental Crystal Structure Determination

2020

Related Article: Luka Ðorđević, Cataldo Valentini, Nicola Demitri, Cécile Mézière, Magali Allain, Marc Sallé, Andrea Folli, Damien Murphy, Samuel Mañas-Valero, Eugenio Coronado, Davide Bonifazi|2020|Angew.Chem.,Int.Ed.|59|4106|doi:10.1002/anie.201914025

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters213-di-t-butyl-69-dichloro-1516-dioxaphenanthro[3456-fghij]pentaphene dibromomethane solvateExperimental 3D Coordinates
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CCDC 1562676: Experimental Crystal Structure Determination

2017

Related Article: György Szalóki, Vincent Croué, Vincent Carré, Frédéric Aubriet, Olivier Alévêque, Eric Levillain, Magali Allain, Juan Aragó, Enrique Ortí, Sébastien Goeb, Marc Sallé|2017|Angew.Chem.,Int.Ed.|56|16272|doi:10.1002/anie.201709483

Space GroupCrystallographyCrystal SystemCrystal Structurebis(mu-44'4''4'''-{(2367-tetrakis(369-trioxadecoxy)anthracene-910-diylidene)bis[(2H-13-dithiole-45-diyl-2-ylidene)]}tetrapyridine)-octakis(35-dichloro-246-trifluorophenyl)-tetra-platinum coronene acetonitrile chloroform solvateCell ParametersExperimental 3D Coordinates
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CCDC 1834563: Experimental Crystal Structure Determination

2018

Related Article: Serhii Krykun, Vincent Croué, Magali Allain, Zoia Voitenko, Juan Aragó, Enrique Ortí, Sébastien Goeb, Marc Sallé|2018|J.Mater.Chem.C|6|13190|doi:10.1039/C8TC04730H

48-bis[45-bis(methylsulfanyl)-2H-13-dithiol-2-ylidene]-48-dihydrobenzo[12-b:45-b']bisthiophene radical cation hexafluorophosphate tetrahydrofuran solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1912053: Experimental Crystal Structure Determination

2020

Related Article: Luka Ðorđević, Cataldo Valentini, Nicola Demitri, Cécile Mézière, Magali Allain, Marc Sallé, Andrea Folli, Damien Murphy, Samuel Mañas-Valero, Eugenio Coronado, Davide Bonifazi|2020|Angew.Chem.,Int.Ed.|59|4106|doi:10.1002/anie.201914025

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters210-di-t-butyl[1]benzopyrano[4'3'2':89]phenanthro[345-mnab]xanthene 210-di-t-butyl[1]benzopyrano[4'3'2':89]phenanthro[345-mnab]xanthene radical hexafluorophosphate tetrahydrofuran solvateExperimental 3D Coordinates
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CCDC 1936956: Experimental Crystal Structure Determination

2020

Related Article: Luka Ðorđević, Cataldo Valentini, Nicola Demitri, Cécile Mézière, Magali Allain, Marc Sallé, Andrea Folli, Damien Murphy, Samuel Mañas-Valero, Eugenio Coronado, Davide Bonifazi|2020|Angew.Chem.,Int.Ed.|59|4106|doi:10.1002/anie.201914025

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(213-di-t-butyl-1516-dioxaphenanthro[3456-fghij]pentaphenium) 213-di-t-butyl-1516-dioxaphenanthro[3456-fghij]pentaphene diperchlorate tetrahydrofuran solvate hemihydrateExperimental 3D Coordinates
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CCDC 1557894: Experimental Crystal Structure Determination

2020

Related Article: Luka Ðorđević, Cataldo Valentini, Nicola Demitri, Cécile Mézière, Magali Allain, Marc Sallé, Andrea Folli, Damien Murphy, Samuel Mañas-Valero, Eugenio Coronado, Davide Bonifazi|2020|Angew.Chem.,Int.Ed.|59|4106|doi:10.1002/anie.201914025

210-di-t-butyl[1]benzopyrano[4'3'2':89]phenanthro[345-mnab]xantheneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1562675: Experimental Crystal Structure Determination

2017

Related Article: György Szalóki, Vincent Croué, Vincent Carré, Frédéric Aubriet, Olivier Alévêque, Eric Levillain, Magali Allain, Juan Aragó, Enrique Ortí, Sébastien Goeb, Marc Sallé|2017|Angew.Chem.,Int.Ed.|56|16272|doi:10.1002/anie.201709483

bis(mu-44'4''4'''-{(2367-tetrakis(369-trioxadecoxy)anthracene-910-diylidene)bis[(2H-13-dithiole-45-diyl-2-ylidene)]}tetrapyridine)-octakis(35-dichloro-246-trifluorophenyl)-tetra-platinum acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1834566: Experimental Crystal Structure Determination

2018

Related Article: Serhii Krykun, Vincent Croué, Magali Allain, Zoia Voitenko, Juan Aragó, Enrique Ortí, Sébastien Goeb, Marc Sallé|2018|J.Mater.Chem.C|6|13190|doi:10.1039/C8TC04730H

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters8-[45-bis(methylsulfanyl)-2H-13-dithiol-2-ylidene]benzo[12-b:45-b']bisthiophen-4(8H)-oneExperimental 3D Coordinates
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